Noun:

ਉਰਨਵ, ਆਕਟੋਪਸ, ਫਰਜ਼ੀ, ਲੋਟਾ,

epimer's Usage Examples:

A convenient procedure for the preparation of ketones in high epimeric purity".

the epimerisation between the sugars N-acetylglucosamine and N-acetylmannosamine, which is catalysed by renin-binding.

In stereochemistry, an epimer is one of a pair of diastereomers.

studies showed that a minor secondary metabolite, brevianamide B, has an epimeric center at the spiro-indoxyl quaternary center.

It is the 22R-epimer of budesonide.

An anomer is an epimer at the hemiacetal/hemiketal carbon in a cyclic saccharide, an atom called the anomeric carbon.

This specificity allows researchers to obtain glycosides in high epimeric excess, one example being Wen-Ya Lu"s conversion of D-Glucose to Ethyl.

It is the α epimer of β-zearalenol and along with β-zearalenol is a major metabolite of zearalenone.

An epimer is a stereoisomer that differs in configuration at any single stereogenic center.

additional epimerization step required to account for the presence of the epimeric neosamine B in neomycin B.

ketone and a monoterpene that occurs predominantly in two diastereomeric (epimeric) forms: (−)-α-thujone and (+)-β-thujone.

It is the β epimer of α-zearalenol and along with α-zearalenol is a major metabolite of zearalenone.

ions are unexpectedly fast solvolysis rates and large differences between epimeric esters.